靶向钾通道Kv1.3杀死胶质母细胞瘤细胞

Q1 Medicine Neurosignals Pub Date : 2017-01-01 Epub Date: 2017-09-01 DOI:10.1159/000480643
Elisa Venturini, Luigi Leanza, Michele Azzolini, Stephanie Kadow, Andrea Mattarei, Michael Weller, Ghazaleh Tabatabai, Michael J Edwards, Mario Zoratti, Cristina Paradisi, Ildikò Szabò, Erich Gulbins, Katrin Anne Becker
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引用次数: 39

摘要

背景/目的:胶质母细胞瘤(GBM)是最具侵袭性的癌症之一,在美国和欧洲新诊断的中枢神经系统(CNS)癌症患者中占很高的比例。GBM的主要特征包括侵袭性和侵袭性生长以及对治疗的高耐药性。Kv1.3是shaker家族的一种钾离子通道,在许多癌细胞的线粒体内膜中表达。线粒体Kv1.3的抑制被证明可以诱导几种肿瘤细胞凋亡,其剂量对正常细胞不致死。方法:采用免疫细胞化学、western blotting和电镜技术检测不同胶质瘤细胞系中Kv1.3的表达,分析新合成的靶向线粒体的Kv1.3抑制剂对胶质瘤细胞死亡的诱导作用。最后,我们对患有胶质瘤的小鼠进行了体内研究。结果:Kv1.3在人和鼠GL261、A172和LN308胶质瘤细胞的线粒体中表达。使用新型Kv1.3抑制剂PAPTP或PCARBTP以及氯法齐明治疗可诱导胶质瘤细胞大量死亡,而Psora-4和PAP-1几乎没有效果。然而,体内实验表明,药物在体内对原位脑肿瘤没有作用。结论:这些数据原则上证明了Kv1.3抑制剂可以杀死GBM细胞,但必须开发出在体内对胶质母细胞瘤起作用的药物,才能在体内转化这些发现。
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Targeting the Potassium Channel Kv1.3 Kills Glioblastoma Cells.

Background/aims: Glioblastoma (GBM) is one of the most aggressive cancers, counting for a high number of the newly diagnosed patients with central nervous system (CNS) cancers in the United States and Europe. Major features of GBM include aggressive and invasive growth as well as a high resistance to treatment. Kv1.3, a potassium channel of the shaker family, is expressed in the inner mitochondrial membrane of many cancer cells. Inhibition of mitochondrial Kv1.3 was shown to induce apoptosis in several tumor cells at doses that were not lethal for normal cells.

Methods: We investigated the expression of Kv1.3 in different glioma cell lines by immunocytochemistry, western blotting and electron microscopy and analyzed the effect of newly synthesized, mitochondria-targeted, Kv1.3 inhibitors on the induction of cell death in these cells. Finally, we performed in vivo studies on glioma bearing mice.

Results: Here, we report that Kv1.3 is expressed in mitochondria of human and murine GL261, A172 and LN308 glioma cells. Treatment with the novel Kv1.3 inhibitors PAPTP or PCARBTP as well as with clofazimine induced massive cell death in glioma cells, while Psora-4 and PAP-1 were almost without effect. However, in vivo experiments revealed that the drugs had no effect on orthotopic brain tumors in vivo.

Conclusion: These data serve as proof of principle that Kv1.3 inhibitors kills GBM cells, but drugs that act in vivo against glioblastoma must be developed to translate these findings in vivo.

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来源期刊
Neurosignals
Neurosignals 医学-神经科学
CiteScore
3.40
自引率
0.00%
发文量
3
审稿时长
>12 weeks
期刊介绍: Neurosignals is an international journal dedicated to publishing original articles and reviews in the field of neuronal communication. Novel findings related to signaling molecules, channels and transporters, pathways and networks that are associated with development and function of the nervous system are welcome. The scope of the journal includes genetics, molecular biology, bioinformatics, (patho)physiology, (patho)biochemistry, pharmacology & toxicology, imaging and clinical neurology & psychiatry. Reported observations should significantly advance our understanding of neuronal signaling in health & disease and be presented in a format applicable to an interdisciplinary readership.
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